| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58475781-58475883 | Rare:44 | ||||
| chr19:58475923-58476494 | Common:4; Rare:201 | ||||
| chr19:58499197-58499685 | Common:3; Rare:174; Clinvar:8; Clinvar (benign):2 | ||||
| chr19:58519731-58520098 | Rare:91 | ||||
| chr19:58543932-58544079 | Rare:40 | ||||
| chr19:58544096-58544505 | Common:5; Rare:177 | ||||
| chr19:58554864-58555460 | Common:3; Rare:180 | ||||
| chr19:58558603-58558745 | Rare:41 | ||||
| chr19:58558829-58559259 | Common:2; Rare:134 | ||||
| chr19:58559439-58559813 | Common:3; Rare:73 | ||||
| chr19:58572665-58573078 | Common:2; Rare:124 | ||||
| chr19:58573268-58573505 | Rare:60 | ||||
| chr2:264752-265015 | Common:1; Rare:137 | ||||
| chr2:677120-677662 | Common:5; Rare:227 | ||||
| chr2:3377129-3377464 | Common:1; Rare:61 |